Variant report

Variant	nsv1026200
Chromosome Location	chr6:35507179-35568562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1115)
CpG islands
(count:551)
Chromatin interactive
region (count:103)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:35521071-35521413	K562	blood:	n/a	n/a
2	ATF3	chr6:35521065-35521374	K562	blood:	n/a	n/a
3	BACH1	chr6:35551696-35551950	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:35536859-35536989	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:35526391-35526712	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:35551549-35551976	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:35527538-35527879	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:35527674-35527807	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:35527664-35527871	K562	blood:	n/a	n/a
10	BHLHE40	chr6:35526387-35526609	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:35551643-35551905	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:35551734-35551963	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:35551619-35551936	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr6:35564154-35565713	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:35534458-35534943	K562	blood:	n/a	n/a
16	CBX3	chr6:35534503-35534821	K562	blood:	n/a	n/a
17	CBX3	chr6:35518128-35518651	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:35520960-35521489	K562	blood:	n/a	n/a
19	CBX3	chr6:35518217-35518567	K562	blood:	n/a	n/a
20	CBX3	chr6:35564233-35565389	HCT-116	colon:	n/a	n/a
21	CBX3	chr6:35519991-35520537	K562	blood:	n/a	n/a
22	CBX3	chr6:35536707-35537063	K562	blood:	n/a	n/a
23	CBX3	chr6:35519985-35520460	K562	blood:	n/a	n/a
24	CBX3	chr6:35518192-35518630	K562	blood:	n/a	n/a
25	CEBPB	chr6:35564151-35565362	HCT-116	colon:	n/a	n/a
26	CEBPB	chr6:35534664-35534908	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:35551752-35551992	HepG2	liver:	n/a	chr6:35551932-35551943
28	CEBPB	chr6:35564079-35565444	HCT-116	colon:	n/a	n/a
29	CEBPB	chr6:35512717-35512917	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:35551716-35551985	H1-hESC	embryonic stem cell:	n/a	chr6:35551932-35551943
31	CEBPB	chr6:35512597-35513014	MCF-7	breast:	n/a	n/a
32	CHD1	chr6:35533324-35533784	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr6:35551676-35552048	GM12878	blood:	n/a	n/a
34	CHD1	chr6:35534176-35534753	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr6:35536884-35537013	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:35534696-35534896	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr6:35521009-35521553	K562	blood:	n/a	n/a
38	CREB1	chr6:35521039-35521540	K562	blood:	n/a	n/a
39	CTCF	chr6:35520160-35520310	GM12875	blood:	n/a	n/a
40	CTCF	chr6:35551549-35552031	A549	lung:	n/a	n/a
41	CTCF	chr6:35551640-35551790	HL-60	blood:	n/a	n/a
42	CTCF	chr6:35536860-35537010	AG09319	gingival:	n/a	chr6:35536914-35536932 chr6:35536917-35536930
43	CTCF	chr6:35520478-35520576	GM19240	blood:	n/a	n/a
44	CTCF	chr6:35520030-35520396	K562	blood:	n/a	n/a
45	CTCF	chr6:35536866-35536970	GM20000	blood:	n/a	chr6:35536914-35536932 chr6:35536917-35536930
46	CTCF	chr6:35536840-35536990	GM12875	blood:	n/a	chr6:35536914-35536932 chr6:35536917-35536930
47	CTCF	chr6:35551662-35551900	LNCaP	prostate:	n/a	n/a
48	CTCF	chr6:35520160-35520310	NHLF	lung:	n/a	n/a
49	CTCF	chr6:35551660-35551810	GM12878	blood:	n/a	n/a
50	CTCF	chr6:35536790-35537050	GM12878	blood:	n/a	chr6:35536914-35536932 chr6:35536917-35536930 chr6:35536795-35536813 chr6:35536798-35536807

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35523735-35523785	HCT-116	colon:	n/a
2	chr6:35543610-35543660	MCF10A-Er-Src	breast:	n/a
3	chr6:35523735-35523785	HCT-116	colon:	n/a
4	chr6:35543610-35543660	MCF10A-Er-Src	breast:	n/a
5	chr6:35523658-35523708	U87	brain:	n/a
6	chr6:35523658-35523708	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:35565116-35565166	HEEpiC	esophagus:	n/a
8	chr6:35551932-35551982	SK-N-SH_RA	brain:	n/a
9	chr6:35523700-35523750	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:35544468-35544518	SK-N-SH	brain:	n/a
11	chr6:35528127-35528177	HAEpiC	amniotic membrane:	n/a
12	chr6:35523658-35523708	HCT-116	colon:	n/a
13	chr6:35512600-35512650	HCM	heart:	n/a
14	chr6:35544468-35544518	AG04449	skin:	fetal
15	chr6:35565116-35565166	HMEC	breast:	n/a
16	chr6:35543610-35543660	LNCaP	prostate:	n/a
17	chr6:35551932-35551982	NT2-D1	testis:	n/a
18	chr6:35551932-35551982	HMEC	breast:	n/a
19	chr6:35565116-35565166	K562	blood:	n/a
20	chr6:35551932-35551982	PFSK-1	brain:	n/a
21	chr6:35523735-35523785	HRPEpiC	eye:	n/a
22	chr6:35523700-35523750	NHDF-neo	bronchial:	n/a
23	chr6:35565116-35565166	IMR90	lung:	fetal
24	chr6:35565116-35565166	PrEC	prostate:	n/a
25	chr6:35543610-35543660	HEEpiC	esophagus:	n/a
26	chr6:35523700-35523750	SK-N-SH	brain:	n/a
27	chr6:35523658-35523708	AG10803	skin:	n/a
28	chr6:35565116-35565166	ovcar-3	ovarian:	n/a
29	chr6:35543610-35543660	GM12891	blood:	n/a
30	chr6:35523735-35523785	PFSK-1	brain:	n/a
31	chr6:35544468-35544518	HEEpiC	esophagus:	n/a
32	chr6:35551932-35551982	HepG2	liver:	n/a
33	chr6:35565116-35565166	RPTEC	kidney:	n/a
34	chr6:35551932-35551982	SK-N-SH	brain:	n/a
35	chr6:35565116-35565166	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:35523735-35523785	LNCaP	prostate:	n/a
37	chr6:35543610-35543660	Caco-2	colon:	n/a
38	chr6:35512600-35512650	SK-N-SH_RA	brain:	n/a
39	chr6:35543610-35543660	NB4	blood:	n/a
40	chr6:35565116-35565166	MCF10A-Er-Src	breast:	n/a
41	chr6:35523700-35523750	HRCEpiC	kidney:	n/a
42	chr6:35551932-35551982	NH-A	brain:	n/a
43	chr6:35544468-35544518	ECC-1	luminal epithelium:	n/a
44	chr6:35523700-35523750	AoSMC	blood vessel:	n/a
45	chr6:35512600-35512650	GM06990	blood:	n/a
46	chr6:35523700-35523750	CMK	blood:	n/a
47	chr6:35544468-35544518	HRE	kidney:	n/a
48	chr6:35523700-35523750	Hela-S3	cervix:	n/a
49	chr6:35523658-35523708	HCF	heart:	n/a
50	chr6:35543610-35543660	BJ	skin:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:35507266..35509878-chr6:35534285..35536876,2	K562	blood:
2	chr6:35562676..35564352-chr6:35607692..35610435,2	K562	blood:
3	chr6:35551819..35553896-chr6:35653247..35655649,2	MCF-7	breast:
4	chr6:35556174..35558038-chr6:35568074..35570018,2	MCF-7	breast:
5	chr6:35554171..35554825-chr6:35704991..35705599,2	K562	blood:
6	chr6:35536482..35537092-chr6:35652393..35652896,2	MCF-7	breast:
7	chr6:35536496..35537201-chr6:35705517..35706230,2	MCF-7	breast:
8	chr6:35568378..35571092-chr6:35588420..35590433,2	K562	blood:
9	chr6:35567248..35569815-chr6:35570869..35573754,2	MCF-7	breast:
10	chr6:35535585..35537526-chr6:35741367..35743409,2	K562	blood:
11	chr6:35549719..35551472-chr6:35552354..35554696,2	MCF-7	breast:
12	chr17:57921307..57924018-chr6:35566994..35568536,2	MCF-7	breast:
13	chr6:35511057..35513907-chr6:35704750..35707121,2	K562	blood:
14	chr6:35553086..35555479-chr6:35655198..35657034,2	MCF-7	breast:
15	chr6:35547345..35549326-chr6:35549483..35552184,3	K562	blood:
16	chr6:35560229..35562371-chr6:35569812..35572139,2	K562	blood:
17	chr6:35490502..35491010-chr6:35519931..35520659,2	K562	blood:
18	chr6:35551965..35554275-chr6:35558656..35560551,2	K562	blood:
19	chr6:35541842..35544127-chr6:35545380..35547353,2	K562	blood:
20	chr6:35551894..35554347-chr6:35560583..35562663,3	K562	blood:
21	chr6:35529182..35531572-chr6:35702765..35705583,2	K562	blood:
22	chr6:35548128..35549662-chr6:35699570..35701770,2	K562	blood:
23	chr6:35551325..35552296-chr6:35696466..35697031,2	MCF-7	breast:
24	chr6:35551061..35552870-chr6:35703622..35704784,16	K562	blood:
25	chr6:35551359..35552588-chr6:35591933..35592441,3	MCF-7	breast:
26	chr6:35538573..35540221-chr6:35543654..35546464,2	K562	blood:
27	chr6:35538573..35540221-chr6:35543654..35546464,2	K562	blood:
28	chr6:35537206..35539251-chr6:35700274..35702012,2	K562	blood:
29	chr6:35265779..35267633-chr6:35521296..35523516,2	K562	blood:
30	chr6:35531994..35534711-chr6:35560308..35562824,2	K562	blood:
31	chr6:35550214..35554619-chr6:35701768..35705947,7	K562	blood:
32	chr6:35547345..35549326-chr6:35549483..35552184,3	K562	blood:
33	chr6:35559772..35562715-chr6:35563847..35566628,3	K562	blood:
34	chr6:35531994..35534711-chr6:35560308..35562824,2	K562	blood:
35	chr6:35538275..35541551-chr6:35544880..35547832,5	K562	blood:
36	chr6:35525249..35527797-chr6:35704384..35706200,2	MCF-7	breast:
37	chr6:35552807..35554347-chr6:35560592..35562141,2	K562	blood:
38	chr6:35564276..35565997-chr6:35567440..35569324,2	MCF-7	breast:
39	chr6:35536462..35537255-chr6:35703793..35704335,2	MCF-7	breast:
40	chr6:35556174..35558038-chr6:35568074..35570018,2	MCF-7	breast:
41	chr6:35538941..35541321-chr6:35548467..35550147,2	K562	blood:
42	chr6:35557946..35559876-chr6:35570097..35572138,2	K562	blood:
43	chr6:35538941..35541321-chr6:35548467..35550147,2	K562	blood:
44	chr6:35490393..35491197-chr6:35551212..35551959,2	MCF-7	breast:
45	chr6:35566723..35569701-chr6:35703866..35705522,2	K562	blood:
46	chr6:35551377..35552255-chr6:35705016..35705834,3	MCF-7	breast:
47	chr6:35535434..35538308-chr6:35704866..35707033,2	K562	blood:
48	chr6:35519589..35521210-chr6:35531779..35534325,2	K562	blood:
49	chr6:35551333..35552161-chr6:35705001..35705965,6	MCF-7	breast:
50	chr6:35550169..35552984-chr6:35694171..35697898,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL10A-1	chr6:35512409-35512482	ENSG00000228559
2	lnc-RPL10A-1	chr6:35512992-35513446	ENSG00000228559
3	lnc-RPL10A-1	chr6:35512645-35512710	ENSG00000228559

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FKBP5	hsa-miR-21-5p	chr6:35542501-35542522
2	FKBP5	hsa-miR-21-5p	chr6:35543161-35543182

Variant related genes	Relation type
ENSG00000219023	TF binding region
ENSG00000228559	TF binding region
ENSG00000219023	CpG island
ENSG00000228559	CpG island
ENSG00000228559	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000007866	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000219023	chromatin interactions

Extended variants
information (count: 2432 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2432 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2894403	chr6:35507179-35507180	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190391706	chr6:35507211-35507212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74622280	chr6:35507214-35507215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373604841	chr6:35507224-35507225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571175170	chr6:35507232-35507233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2395631	chr6:35507315-35507316	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs553819283	chr6:35507326-35507327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145058726	chr6:35507333-35507334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568010314	chr6:35507336-35507337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76489311	chr6:35507418-35507419	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556028574	chr6:35507478-35507479	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs574309129	chr6:35507528-35507529	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547760943	chr6:35507533-35507534	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs4713888	chr6:35507556-35507557	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs563050556	chr6:35507568-35507569	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577963605	chr6:35507579-35507580	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545120832	chr6:35507630-35507631	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560614514	chr6:35507691-35507692	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs527816626	chr6:35507716-35507717	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377575220	chr6:35507717-35507718	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146805783	chr6:35507776-35507777	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370996241	chr6:35507787-35507788	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140530748	chr6:35507805-35507806	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531406118	chr6:35507809-35507810	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549622499	chr6:35507848-35507849	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552396316	chr6:35507861-35507862	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377137856	chr6:35507873-35507874	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181710445	chr6:35507963-35507964	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557905849	chr6:35508020-35508021	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145655403	chr6:35508081-35508082	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187390222	chr6:35508089-35508090	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536315601	chr6:35508096-35508097	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570527590	chr6:35508136-35508137	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs62402114	chr6:35508209-35508210	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs199827030	chr6:35508214-35508215	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554710907	chr6:35508237-35508238	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs77967936	chr6:35508280-35508281	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539601969	chr6:35508302-35508303	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538483159	chr6:35508358-35508359	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556813746	chr6:35508397-35508398	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148083418	chr6:35508427-35508428	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553216320	chr6:35508435-35508436	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545371233	chr6:35508471-35508472	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566742468	chr6:35508475-35508476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535785856	chr6:35508498-35508499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553846826	chr6:35508513-35508514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11759543	chr6:35508531-35508532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375076380	chr6:35508532-35508533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs9366889	chr6:35508565-35508566	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374586290	chr6:35508605-35508606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35503600-35511200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:35509600-35510200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:35509600-35510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:35509800-35510000	Enhancers	Placenta Amnion	Placenta Amnion
5	chr6:35509800-35510200	Enhancers	Primary hematopoietic stem cells	blood
6	chr6:35510000-35510200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:35510000-35510200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:35510000-35512400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:35510200-35511200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:35510200-35512400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:35510400-35511400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:35511000-35511400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr6:35511000-35511600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr6:35511200-35511400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:35511200-35511400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:35511200-35511400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:35511200-35511400	Bivalent Enhancer	HepG2	liver
18	chr6:35511200-35511600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr6:35511200-35511600	Enhancers	Dnd41	blood
20	chr6:35511200-35511800	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr6:35511200-35511800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:35511200-35511800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr6:35511200-35511800	Enhancers	Fetal Thymus	thymus
24	chr6:35511200-35512600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:35511200-35513400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:35511200-35514200	Enhancers	Placenta	Placenta
27	chr6:35511400-35511600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:35511400-35511600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:35511400-35511600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:35511400-35511600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:35511400-35511600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:35511400-35511800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr6:35511400-35512400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:35511400-35512400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:35511400-35513400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:35511600-35512000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr6:35511600-35512200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr6:35511600-35512400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:35511600-35512800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:35511800-35512000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr6:35511800-35512200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr6:35511800-35512200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr6:35511800-35512400	Weak transcription	Fetal Thymus	thymus
44	chr6:35512000-35512400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:35512000-35513400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr6:35512200-35512400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:35512200-35513200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:35512200-35513200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:35512200-35513400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr6:35512200-35513400	Enhancers	NHEK	skin

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